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Q52877119-06243405-4F5D-4EBC-8C1C-19F4FA0DAE83
Q52877119-06243405-4F5D-4EBC-8C1C-19F4FA0DAE83
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http://www.wikidata.org/entity/statement/Q52877119-06243405-4F5D-4EBC-8C1C-19F4FA0DAE83
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia.
P2860
Q52877119-06243405-4F5D-4EBC-8C1C-19F4FA0DAE83
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Statement
http://www.wikidata.org/entity/statement/Q52877119-06243405-4F5D-4EBC-8C1C-19F4FA0DAE83
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wasDerivedFrom
e63241ed8bea64ec4285612802c67fdd2b4be52f
P2860
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.